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Polycystic ovary syndrome, or polycystic ovarian syndrome (PCOS), is the most common endocrine disorder in women of reproductive age. [14] The syndrome is named after cysts which form on the ovaries of some women with this condition, though this is not a universal symptom and not the underlying cause of the disorder.
Several studies found only weak signs of adaptive evolution early in the COVID-19 pandemic. [c] Kang et al. wrote that SARS-CoV-2 had exhibited relatively little genetic variation by 2021. [47] Tai et al. wrote that population expansion rather than positive selection explained the mutation frequency spectrum during the early pandemic. [49]
The virus' global spread caused the COVID-19 pandemic. [30] Some research suggests that genetic conditions are among the causes of co-morbid conditions that lead to more severe COVID-19 symptoms, such as death. [31] [32] [33] Early in the pandemic, many regions experienced shortages of medical resources like PPE and ventilators. [34]
Hyperandrogenism can appear as a symptom of many different genetic and medical conditions. Some of the conditions with hyperandrogenic symptoms, including PCOS, may sometimes be hereditary. Additionally, it is thought that epigenetics may contribute to the pathogenesis of polycystic ovary syndrome. [55]
The genetic, hormonal, metabolic and reproductive disorder can cause irregular periods, acne, infertility, weight gain and excessive hair growth, according to the PCOS Awareness Month website.
Although this piece references "genetic causes" as an established scientific fact, nothing could be further from the truth, and of the two sources referenced, one is a 2002 paper which talks about a couple of gene loci, but not a genetic cause, and the other reference simply talks about genetic screening technologies but does not say that PCOS ...
Molly Smith experienced pins and needles in her hands and feet, which eventually led to the discovery of a cyst and a diagnosis of ovarian cancer.
The term variant of concern (VOC) for SARS-CoV-2, which causes COVID-19, is a category used for variants of the virus where mutations in their spike protein receptor binding domain (RBD) substantially increase binding affinity (e.g., N501Y) in RBD-hACE2 complex (genetic data), while also being linked to rapid spread in human populations ...